Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798670Generated: November 1, 2026

2-Methyl-3-butyn-2-ol → 4-Hydroxy-1-(4-methoxyphenyl)-4-methylpent-2-yn-1-one

https://huagongshe.com/reaction/1798670

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-3-butyn-2-olHCID 8258—
ReactantN,4-Dimethoxy-N-methylbenzamideHCID 15105748—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-Hydroxy-1-(4-methoxyphenyl)-4-methylpent-2-yn-1-oneHCID 1272257781%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a stirred solution of 2-methylbut-3-yn-2-ol (2.15 g, 25.6 mmol) in dry THF (80 mL) was added n-BuLi (24.0 mL, 38.7 mmol, 1.6 M in hexane) drop wise at −20° C. under an inert atmosphere for a period of 10 min. After being stirred for 30 min at −20° C., a solution of N,4-dimethoxy-N-methylbenzamide (2.5 g, 12.8 mmol) in dry THF (10 mL) was added to reaction mixture and stirring was continued for an additional 3 h at −20° C. The reaction mixture was quenched with a saturated NH4Cl solution and extracted with EtOAc (2×100 mL). The combined organic layer was washed with water (100 mL), brine (40 mL), dried over Na2SO4, filtered and concentrated in vacuo to afford 4-hydroxy-1-(4-methoxyphenyl)-4-methylpent-2-yn-1-one (2.25 g, 81%) as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343973B2
Source datasetuspto-grants-2013_01
ORD IDord-c387af050c57463bb4781fbf52993b46
Source noteuspto-grants-2013_01